SynonymsGirl affected by trichorhinophalangeal syndrome type 1 (TRPS1)

TRPSI

Trichorhinophalangeal Syndrome, Type 1 (TRPS1) is a Rare Genetic Condition Characterized by the Following Symptoms and Features


Growth

  • Short stature
  • Normal birth length
  • Mild growth deficiency

Face

  • Prominent, long vertical groove in the middle area above the upper lip (philtrum)
  • Very small lower jaw (micrognathia)
  • Horizontal groove on chin

Ears

  • Large, prominent

Eyes

  • Thin eyebrows (laterally)

Nose

  • Pear-shaped

Mouth

  • Narrow palate
  • Thin upper lip

Teeth

  • Small
  • Carious (cavities, tooth decay)
  • Not aligned properly (dental malocclusion)
  • Late having teeth come in (delayed teeth eruption)

Respiratory

  • Recurrent respiratory infections

Chest

  • The shoulder blade, or shoulder bone, protrudes from a person’s back in an abnormal position (winged scapulae)
  • Pectus carinatum (keel-shaped deformity of the chest, protrusion abnormalities of the anterior chest wall)

Skeletal

  • Delayed bone age before puberty (slow bone growth)
  • Accelerated bone age after puberty
  • Osteopenia (late-onset) (lower than normal bone density)
  • Osteoarthritis (late-onset)
  • Joint pain (late-onset)

Spine

  • Spine has a sideways curve. The curve is usually “S” or “C” shaped. (scoliosis)
  • Excessive curvature of the lower back (lordosis)

Pelvis

  • Deformities in the large bone in the leg/ femur

Hands

  • Short and misshapen fingers

Feet

  • Flat foot
  • Short toes

Nails

  • Thin
  • Spoon shaped
  • White spots

Hair

  • Sparse
  • Thin
  • Slow growing
  • Thin eyebrows

Neurological

  • Low muscle tone in infancy (hypotonia)
  • Normal intelligence

Voice

  • Deep 

Diagnosing

Trichorhinophalangeal syndrome, type 1 is best diagnosed by a geneticist with genetic testing.

Causes

TRPS1 is caused by changes in the zinc finger transcription factor TRPS1.

Genetic Testing

There is a genetic test for TRPS1. Find more resources about genetic testing, including costs, benefits and risks from Genes In Life.

Inheritance

TRPS1 is inherited as an autosomal dominant disorder. An affected individual has a 50% chance of passing the TRPS1 gene to a son or daughter.

Learn more about TRPS1 at Online Mendelian Inheritance in Man.